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United Hip System

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
United Hip System FDA UDI
Generic Name
Metal-on-polyethylene total hip prosthesis FDA UDI
Device Name
Conformity Stem,#0 FDA UDI
Model / Reference
1110-3000 FDA UDI
Description
Conformity Stem,#0 FDA UDI

Identifiers

Primary DI / UDI-DI
04719886901177 FDA UDI
510(k) Number
K243466 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
GMDN Term
Metal-on-polyethylene total hip prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Metal-on-polyethylene total hip prosthesis

United Hip System by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metal-on-polyethylene total hip prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c84930f8-bbe7-4068-be4c-2db88a6e7e09 35 fields · synced May 30, 2026